List of variants in gene IMPA1 reported as uncertain significance for Intellectual disability, autosomal recessive 59

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005536.4(IMPA1):c.379G>C (p.Glu127Gln)	rs376742471	0.00014
NM_005536.4(IMPA1):c.613A>G (p.Thr205Ala)	rs149824165	0.00001
NM_005536.4(IMPA1):c.719G>A (p.Gly240Asp)	rs1260261553

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